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首页> 外文期刊>Infection control and hospital epidemiology >Sterility and microbiological assessment of reused single-use cardiac electrophysiology catheters.
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Sterility and microbiological assessment of reused single-use cardiac electrophysiology catheters.

机译:重复使用的一次性心脏电生理导管的无菌性和微生物学评估。

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摘要

OBJECTIVE: To assess the performance and limitations of a reprocessing protocol for nonlumen electrophysiology catheters by testing the sterility of reprocessed devices and defining the maximum number of reprocessing cycles sustainable by the device in hygienically safe conditions. DESIGN: Simulated use, reprocessing, and testing of the catheters. SETTING: Microbiology and virology department of a public health diagnostic laboratory. INTERVENTIONS: Seventy-three catheters were collected after clinical use on patients. The first group of devices was tested for sterility after 1 cycle of reprocessing. By the repetition of simulated use (blood inoculated with bacteria) and reprocessing (decontamination, cleaning, and hydrogen peroxide gas plasma sterilization), we obtained 39 sample devices reprocessed 2 times, 26 reprocessed 3 times, 28 reprocessed 4 times, 36 reprocessed 5 times, and 22 reprocessed 6 times. Devices were cultured for 28 days in trypticase soy broth. RESULTS: We tested 208 catheters with 6 cycles of reprocessing and 4 inoculated bacteria species. No devices tested positive for the inoculated strains until the fourth cycle of reprocessing. One of 35 catheters showed the growth of the inoculated strain Bacillus subtilis after 5 cycles of reprocessing, and 1 of 22 catheters showed growth of this organism 6 cycles. After the second reprocessing, 7 of 36 devices showed growth of gram-negative bacteria other than the strain inoculated. CONCLUSIONS: Reprocessing according to the reprocessing protocol was insufficient to guarantee device sterility after 5 reuses. Cleaning with enzymatic solution revealed good cleaning properties with efficient bioburden reduction. Storage intervals of longer than 24 hours during reprocessing should be avoided to limit contamination or bacterial overgrowth. Technical considerations suggest the introduction of reprocessing procedures only in hospitals with considerable workloads.
机译:目的:通过测试再处理装置的无菌性并定义在卫生安全的条件下该装置可承受的最大再处理循环次数,以评估非内腔电生理导管再处理协议的性能和局限性。设计:模拟使用,再加工和测试导管。单位:公共卫生诊断实验室的微生物学和病毒学部门。干预措施:对患者进行临床使用后收集了73条导管。在经过1个周期的再处理后,对第一组设备进行了无菌测试。通过重复模拟使用(血液接种细菌)和再处理(去污,清洁和过氧化氢气体等离子体灭菌),我们获得了39个样品设备,分别进行了2次重复处理,26次重复处理3次,28次重复处理4次,36次重复处理5次,并且22被重新处理了6次。将设备在胰蛋白酶大豆肉汤中培养28天。结果:我们测试了208个导管,进行了6个循环的后处理和4种接种的细菌种类。直到再加工的第四个周期,才有设备对接种的菌株测试呈阳性。 35个导管中的一个显示了经过5个循环后接种的枯草芽孢杆菌菌株的生长,而22个导管中的一个显示了6个周期的生长。第二次再处理后,36个设备中有7个显示出除所接种菌株以外的革兰氏阴性细菌的生长。结论:根据再处理协议进行的再处理不足以保证5次再使用后设备的无菌性。用酶溶液清洗显示出良好的清洗性能,并有效降低了生物负荷。在后处理期间,应避免超过24小时的存储间隔,以限制污染或细菌过度生长。技术方面的考虑建议仅在工作量很大的医院中采用后处理程序。

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